Synfacts 2023; 19(11): 1169
DOI: 10.1055/s-0042-1751613
Peptide Chemistry

Organocatalyzed Enantioselective Synthesis of α-Amino Acids

Rezensent(en):
Hisashi Yamamoto
,
Isai Ramakrishna
Lygo B, *, Wainwright PG. University of Salford, UK
A New Class of Asymmetric Phase-Transfer Catalysts Derived from Cinchona Alkaloids – Application in the Enantioselective Synthesis of α-Amino Acids.

Tetrahedron Lett. 1997;
38: 8595-8598
 

Significance

Unnatural amino acids play a unique role in the peptide drug development ­arena. Hence, peptide development chemists are highly attracted to the development of new methods for the synthesis of unnatural amino acids. In 1997, the authors developed a new method for the synthesis of optically pure amino acids using a cinchona ­alkaloid-derived phase-transfer catalyst.


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Comment

A series of unnatural α-amino acids were synthesized by asymmetric alkylation of a benzophenone-derived glycine imine with the help of a cinchona alkaloid-derived phase-transfer catalyst. The reaction could produce α-amino acids with moderate to good optical purity.


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Publikationsverlauf

Artikel online veröffentlicht:
14. Oktober 2023

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